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Evaluating Potential Risk of Choking by Laryngeal Ultrasound in Patients With Acute Stroke

Not Applicable
Recruiting
Conditions
Acute Stroke
Interventions
Diagnostic Test: ultrasound
Registration Number
NCT04874454
Lead Sponsor
National Taiwan University Hospital
Brief Summary

The investigators evaluate the vocal cord movement in patients with acute stroke by ultrasound. The occurrence of choking or aspiration pneumonia will be collected in one year after the index stroke.

Detailed Description

Post-stroke dysphagia is a common complication for the stroke patient. It may cause aspiration, poor nutrition or even pneumonia; thus, it is crucial for the physicians to evaluate the swallowing function of the stroke patients. However, the evaluation methods nowadays still have some limitations. Water swallowing test is one of the well-known methods, but the test itself would put the patients at risk of aspiration. Furthermore, in order to increase the sensitivity of the water swallowing test, the amount of the water should also be increased; as a consequence, the risk of aspiration will also increase. Fiberoptic endoscopic evaluation of the swallowing and videofluoroscopy have limitations of invasiveness. The laryngeal ultrasound to evaluate the vocal cord movement can be an alternative method, having the characteristics of non-invasiveness and repeat evaluation.

The investigators aim to evaluate the vocal cord movement in patients with acute stroke by ultrasound. The occurrence of choking or aspiration pneumonia will be collected in one year after the index stroke.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • acute stroke (in one month) patients
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Exclusion Criteria
  • patients with stroke occurring more than one month ago
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
vocal cord movement among the stroke patientsultrasound-
Primary Outcome Measures
NameTimeMethod
the incidence of aspiration pneumoniaone year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Wan-Ching Lien

🇨🇳

Taipei, None Selected, Taiwan

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